| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:56300003-56300147 | Common:2; Rare:57 | ||||
| chr12:56315131-56315456 | Rare:92 | ||||
| chr12:56315823-56316105 | Common:1; Rare:69 | ||||
| chr12:56449334-56449734 | Rare:73 | ||||
| chr12:56642515-56642694 | Rare:45 | ||||
| chr12:56688081-56688598 | Common:5; Rare:173 | ||||
| chr12:56752310-56752491 | Rare:56 | ||||
| chr12:57111160-57111425 | Common:4; Rare:48 | ||||
| chr12:57720250-57720514 | Rare:91 | ||||
| chr12:57772087-57772239 | Rare:55 | ||||
| chr12:57782667-57782797 | Rare:44; Clinvar (benign):1 | ||||
| chr12:62260059-62260432 | Common:1; Rare:137 | ||||
| chr12:64222261-64222349 | Rare:23 | ||||
| chr12:64404223-64404556 | Common:2; Rare:126 | ||||
| chr12:64759097-64759482 | Rare:124; Clinvar:6; Clinvar (benign):2 |